DOP2018000065A - DERIVATIVES OF 8- [6- [3- (AMINO) PROPOXI] -3-PIRIDIL] 1-ISOPROPILIMIDAZO [4,5-C] QUINOLIN-2-ONA AS SELECTED MODULATORS OF THE MUTED TELANGIECTASIA ATAXIA KINASE (ATM) FOR THE CANCER TREATMENT - Google Patents
DERIVATIVES OF 8- [6- [3- (AMINO) PROPOXI] -3-PIRIDIL] 1-ISOPROPILIMIDAZO [4,5-C] QUINOLIN-2-ONA AS SELECTED MODULATORS OF THE MUTED TELANGIECTASIA ATAXIA KINASE (ATM) FOR THE CANCER TREATMENTInfo
- Publication number
- DOP2018000065A DOP2018000065A DO2018000065A DO2018000065A DOP2018000065A DO P2018000065 A DOP2018000065 A DO P2018000065A DO 2018000065 A DO2018000065 A DO 2018000065A DO 2018000065 A DO2018000065 A DO 2018000065A DO P2018000065 A DOP2018000065 A DO P2018000065A
- Authority
- DO
- Dominican Republic
- Prior art keywords
- quinolin
- atm
- isopropilimidazo
- propoxi
- piridil
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
La memoria descriptiva se refiere en general a compuestos de Fórmula (I): (I) y sales farmacéuticamente aceptables de estos, donde R1, R2, R3, R4 y R5 tienen cualquiera de los significados definidos en la presente. La memoria descriptiva también se refiere al uso de compuestos de Fórmula (I) y sales de estos para tratar o prevenir una enfermedad mediada por ATM, incluido el cáncer. La memoria descriptiva se refiere además a composiciones farmacéuticas que comprenden compuestos de tipo imidazo[4,5-c]quinolin-2-ona sustituidos y sales farmacéuticamente aceptables de estos; kits que comprenden tales compuestos y sales; métodos de producción de tales compuestos y sales; e intermedios útiles en tal producción.The specification refers in general to compounds of Formula (I): (I) and pharmaceutically acceptable salts thereof, where R1, R2, R3, R4 and R5 have any of the meanings defined herein. The specification also refers to the use of compounds of Formula (I) and salts thereof to treat or prevent an ATM-mediated disease, including cancer. The specification also relates to pharmaceutical compositions comprising imidazo [4,5-c] quinolin-2-one substituted compounds and pharmaceutically acceptable salts thereof; kits comprising such compounds and salts; production methods of such compounds and salts; and intermediates useful in such production.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB1516504.6A GB201516504D0 (en) | 2015-09-17 | 2015-09-17 | Imadazo(4,5-c)quinolin-2-one Compounds and their use in treating cancer |
Publications (1)
Publication Number | Publication Date |
---|---|
DOP2018000065A true DOP2018000065A (en) | 2018-03-30 |
Family
ID=54544418
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DO2018000065A DOP2018000065A (en) | 2015-09-17 | 2018-03-06 | DERIVATIVES OF 8- [6- [3- (AMINO) PROPOXI] -3-PIRIDIL] 1-ISOPROPILIMIDAZO [4,5-C] QUINOLIN-2-ONA AS SELECTED MODULATORS OF THE MUTED TELANGIECTASIA ATAXIA KINASE (ATM) FOR THE CANCER TREATMENT |
Country Status (37)
Country | Link |
---|---|
US (5) | US9856255B2 (en) |
EP (2) | EP3683220B1 (en) |
JP (1) | JP6605130B2 (en) |
KR (2) | KR102469153B1 (en) |
CN (1) | CN108137576B (en) |
AR (1) | AR106053A1 (en) |
AU (1) | AU2016323399B2 (en) |
BR (1) | BR112018004325B1 (en) |
CA (1) | CA2997399C (en) |
CL (1) | CL2018000677A1 (en) |
CO (1) | CO2018002829A2 (en) |
CR (1) | CR20180172A (en) |
CY (1) | CY1124680T1 (en) |
DK (2) | DK3683220T3 (en) |
DO (1) | DOP2018000065A (en) |
EA (1) | EA033284B1 (en) |
ES (2) | ES2853924T3 (en) |
GB (1) | GB201516504D0 (en) |
HK (2) | HK1255408A1 (en) |
HR (1) | HRP20210149T1 (en) |
HU (2) | HUE053066T2 (en) |
IL (1) | IL257847B (en) |
LT (1) | LT3350180T (en) |
MX (1) | MX2018003186A (en) |
MY (1) | MY195669A (en) |
NI (1) | NI201800033A (en) |
PE (1) | PE20181078A1 (en) |
PH (1) | PH12018500532A1 (en) |
PL (2) | PL3350180T3 (en) |
PT (2) | PT3683220T (en) |
RS (1) | RS61435B1 (en) |
SI (1) | SI3350180T1 (en) |
SV (1) | SV2018005655A (en) |
TN (1) | TN2018000078A1 (en) |
TW (2) | TWI714631B (en) |
WO (1) | WO2017046216A1 (en) |
ZA (1) | ZA202209171B (en) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB201516504D0 (en) * | 2015-09-17 | 2015-11-04 | Astrazeneca Ab | Imadazo(4,5-c)quinolin-2-one Compounds and their use in treating cancer |
GB201608227D0 (en) * | 2016-05-11 | 2016-06-22 | Astrazeneca Ab | Imidazo[4,5-c]quinolin-2-one compounds and their use in treating cancer |
JOP20190209A1 (en) * | 2017-03-16 | 2019-09-12 | Astrazeneca Ab | Deuterated imidazo[4,5-c]quinolin-2-one compounds and their use in treating cancer |
CN111344293A (en) | 2017-09-20 | 2020-06-26 | 阿斯利康(瑞典)有限公司 | 1, 3-dihydroimidazo [4, 5-c ] cinnolin-2-one compounds and their use in the treatment of cancer |
WO2020052688A1 (en) | 2018-09-14 | 2020-03-19 | Suzhou Zanrong Pharma Limited | 1-ISOPROPYL-3-METHYL-8- (PYRIDIN-3-YL) -1, 3-DIHYDRO-2H-IMIDAZO [4, 5-c] CINNOLIN-2-ONE AS SELECTIVE MODULATORS OF ATAXIA TELANGIECTASIA MUTATED (ATM) KINASE AND USES THEREOF |
WO2021139814A1 (en) * | 2020-01-09 | 2021-07-15 | 南京明德新药研发有限公司 | Quinoline imidazole compound and application thereof |
US20230293507A1 (en) * | 2020-03-04 | 2023-09-21 | Pharos Ibio Co., Ltd | Use of 2,3,5-substituted thiophene compound for preventing, ameliorating, or treating ovarian cancer |
JP2023539715A (en) | 2020-06-24 | 2023-09-19 | アストラゼネカ ユーケー リミテッド | Combination of antibody-drug conjugates and ATM inhibitors |
EP4219499A1 (en) * | 2020-09-28 | 2023-08-02 | CSPC Zhongqi Pharmaceutical Technology (Shijiazhuang) Co., Ltd. | A class of fused ring compounds, and preparation and use thereof |
EP3992191A1 (en) | 2020-11-03 | 2022-05-04 | Deutsches Krebsforschungszentrum | Imidazo[4,5-c]quinoline compounds and their use as atm kinase inhibitors |
WO2022125614A1 (en) * | 2020-12-09 | 2022-06-16 | Stingray Therapeutics, Inc. | Phosphonates as inhibitors of enpp1 and cdnp |
AU2021433713A1 (en) * | 2021-03-17 | 2023-09-28 | Suzhou Zanrong Pharma Limited | Selective modulators of ataxia telangiectasia mutated (atm) kinase and uses thereof |
CN115304598B (en) * | 2021-08-25 | 2024-05-31 | 石药集团中奇制药技术(石家庄)有限公司 | Heterocyclic compound, and preparation method and application thereof |
GB202114704D0 (en) | 2021-10-14 | 2021-12-01 | Univ Birmingham | ATM inhibition |
IL314381A (en) * | 2022-01-26 | 2024-09-01 | Chia Tai Tianqing Pharmaceutical Group Co Ltd | Hydrazino group-containing compound |
WO2023200427A1 (en) * | 2022-04-11 | 2023-10-19 | Wei Zhong | Substituted 1-(3,3-difluoropiperidin-4-yl)-imidazo[4,5-c] quinolin-2-one derivative crystal form, salt crystal form, preparation method and application |
Family Cites Families (92)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NZ240313A (en) | 1990-10-22 | 1994-04-27 | Res Corp Technologies Inc | Anti-retrovirus compositions containing aryl and heteroaryl derivatives |
TW301607B (en) | 1993-03-09 | 1997-04-01 | Takeda Pharm Industry Co Ltd | |
GB9624482D0 (en) | 1995-12-18 | 1997-01-15 | Zeneca Phaema S A | Chemical compounds |
KR19990082463A (en) | 1996-02-13 | 1999-11-25 | 돈 리사 로얄 | Quinazolin derivatives as vascular endothelial growth factor inhibitors |
CN1116286C (en) | 1996-03-05 | 2003-07-30 | 曾尼卡有限公司 | 4-anilinoquinazoline derivatives |
GB9718972D0 (en) | 1996-09-25 | 1997-11-12 | Zeneca Ltd | Chemical compounds |
US6632823B1 (en) | 1997-12-22 | 2003-10-14 | Merck & Co., Inc. | Substituted pyridine compounds useful as modulators of acetylcholine receptors |
JP2002522388A (en) | 1998-08-03 | 2002-07-23 | ビーエーエスエフ コーポレーション | Pyridinone for the treatment of sexual dysfunction |
EP1150955A2 (en) | 1999-02-04 | 2001-11-07 | Millennium Pharmaceuticals, Inc. | G-protein coupled heptahelical receptor binding compounds and methods of use thereof |
US20020151712A1 (en) | 1999-09-14 | 2002-10-17 | Nan-Horng Lin | 3-pyrrolidinyloxy-3'-pyridyl ether compounds useful for controlling chemical synaptic transmission |
WO2002030357A2 (en) | 2000-10-11 | 2002-04-18 | Chemocentryx, Inc. | Compounds and methods for modulating ccr4 function |
AU2002213467A1 (en) | 2000-10-11 | 2002-04-22 | Chemocentryx, Inc. | Modulation of ccr4 function |
EP1217000A1 (en) | 2000-12-23 | 2002-06-26 | Aventis Pharma Deutschland GmbH | Inhibitors of factor Xa and factor VIIa |
WO2002076177A2 (en) | 2001-03-23 | 2002-10-03 | Bethesda Pharmaceuticals, Inc. | Design and synthesis of optimized ligands for ppar |
JP2002293745A (en) | 2001-03-29 | 2002-10-09 | St Marianna Univ School Of Medicine | Therapeutic agent for chronic rheumatism |
CA2442654A1 (en) | 2001-04-10 | 2002-10-10 | Transtech Pharma, Inc. | Probes, systems, and methods for drug discovery |
WO2002087618A1 (en) | 2001-04-27 | 2002-11-07 | Takeda Chemical Industries, Ltd. | Preventive/therapeutic method for cancer |
WO2002094264A1 (en) | 2001-05-23 | 2002-11-28 | Tularik Inc. | Ccr4 antagonists |
EP1270535A3 (en) | 2001-06-20 | 2004-02-18 | Clariant GmbH | Method to synthesise substituted aromatic compounds |
JP4082888B2 (en) | 2001-10-17 | 2008-04-30 | 広栄化学工業株式会社 | Process for producing biaryl compounds |
WO2003062392A2 (en) | 2002-01-18 | 2003-07-31 | Ceretek Llc | Methods of treating conditions associated with an edg receptor |
JP4167848B2 (en) | 2002-04-10 | 2008-10-22 | 広栄化学工業株式会社 | Process for producing biaryl compounds |
GB0211649D0 (en) | 2002-05-21 | 2002-07-03 | Novartis Ag | Organic compounds |
US20060004010A1 (en) | 2002-07-10 | 2006-01-05 | Hiromu Habashita | Ccr4 antagonist and medical use thereof |
CN1678303A (en) | 2002-08-23 | 2005-10-05 | 康涅狄格大学 | Keto cannabinoids with therapeutic indications |
US20040087590A1 (en) | 2002-08-23 | 2004-05-06 | University Of Connecticut | Novel biphenyl and biphenyl-like cannabinoids |
EP1599475A2 (en) | 2003-03-06 | 2005-11-30 | Eisai Co., Ltd. | Jnk inhibitors |
WO2004080943A1 (en) | 2003-03-11 | 2004-09-23 | Ono Pharmaceutical Co., Ltd. | Cinnamyl alcohol derivative compounds and drugs containing the compounds as the active ingredient |
WO2004113258A1 (en) | 2003-06-20 | 2004-12-29 | Shionogi & Co., Ltd. | Carbon-carbon bond forming reaction |
JPWO2005023771A1 (en) | 2003-09-05 | 2006-11-02 | 小野薬品工業株式会社 | Chemokine receptor antagonist and its pharmaceutical use |
JP2005170939A (en) | 2003-11-20 | 2005-06-30 | Takeda Chem Ind Ltd | Prophylactic/therapeutic agent for diabetes |
KR20060117329A (en) | 2003-11-21 | 2006-11-16 | 노파르티스 아게 | 1h-imidazoquinoline derivatives as protein kinase inhibitors |
WO2006038594A1 (en) | 2004-10-04 | 2006-04-13 | Ono Pharmaceutical Co., Ltd. | N-type calcium channel inhibitor |
JP4318087B2 (en) | 2004-12-13 | 2009-08-19 | 小野薬品工業株式会社 | Aminocarboxylic acid derivatives and their pharmaceutical use |
GB0510390D0 (en) | 2005-05-20 | 2005-06-29 | Novartis Ag | Organic compounds |
US20070032522A1 (en) | 2005-07-01 | 2007-02-08 | Kumar Dange V | Antiviral agents |
EP1962861A2 (en) | 2005-08-26 | 2008-09-03 | Emory University | Compounds and methods for modulating the silencing of a polynucleotide of interest |
JO3598B1 (en) | 2006-10-10 | 2020-07-05 | Infinity Discovery Inc | Boronic acids and esters as inhibitors of fatty acid amide hydrolase |
JP2009023986A (en) | 2006-11-08 | 2009-02-05 | Pharma Ip | Biaryl derivative as anticancer agent |
CL2008000191A1 (en) | 2007-01-25 | 2008-08-22 | Astrazeneca Ab | COMPOUNDS DERIVED FROM 4-AMINO-CINNOTINA-3-CARBOXAMIDA; CSF-1R QUINASA INHIBITORS; YOUR PREPARATION PROCESS; AND ITS USE TO TREAT CANCER. |
US9370508B2 (en) | 2007-02-20 | 2016-06-21 | Novartis Ag | Imidazoquinolines as dual lipid kinase and mTOR inhibitors |
JP2010520293A (en) | 2007-03-07 | 2010-06-10 | アラントス・フアーマシユーテイカルズ・ホールデイング・インコーポレイテツド | Metalloprotease inhibitors containing heterocyclic moieties |
US8039505B2 (en) | 2007-04-11 | 2011-10-18 | University Of Utah Research Foundation | Compounds for modulating T-cells |
PE20090717A1 (en) | 2007-05-18 | 2009-07-18 | Smithkline Beecham Corp | QUINOLINE DERIVATIVES AS PI3 KINASE INHIBITORS |
US7928111B2 (en) | 2007-06-08 | 2011-04-19 | Senomyx, Inc. | Compounds including substituted thienopyrimidinone derivatives as ligands for modulating chemosensory receptors |
US9321730B2 (en) | 2007-08-21 | 2016-04-26 | The Hong Kong Polytechnic University | Method of making and administering quinoline derivatives as anti-cancer agents |
CN101980708B (en) | 2008-03-26 | 2013-03-13 | 诺瓦提斯公司 | Imidazoquinolines and pyrimidine derivatives as potent modulators of VEGF-driven angiogenic processes |
AU2009266956B2 (en) | 2008-07-01 | 2014-03-20 | Genentech, Inc. | Bicyclic heterocycles as MEK kinase inhibitors |
TW201028381A (en) | 2008-07-14 | 2010-08-01 | Shionogi & Co | Pyridine derivative having ttk inhibition activity |
US8791131B2 (en) | 2008-09-30 | 2014-07-29 | Pfizer Inc. | Imidazo[1,5]naphthyridine compounds, their pharmaceutical use and compositions |
WO2010077680A2 (en) | 2008-12-08 | 2010-07-08 | Vm Discovery Inc. | Compositions of protein receptor tyrosine kinase inhibitors |
US20120093917A1 (en) | 2009-04-02 | 2012-04-19 | Robert Hromas | Metnase and intnase inhibitors and their use in treating cancer |
TW201041888A (en) | 2009-05-06 | 2010-12-01 | Plexxikon Inc | Compounds and methods for kinase modulation, and indications therefor |
MX2011012943A (en) * | 2009-06-04 | 2012-01-27 | Novartis Ag | 1H-IMIDAZO[4,5-c]QUINOLINONE DERIVATIVES. |
WO2010139747A1 (en) * | 2009-06-04 | 2010-12-09 | Novartis Ag | 1H-IMIDAZO[4, 5-c]QUINOLINONE COMPOUNDS, USEFUL FOR THE TREATMENT OF PROLIFERATIVE DISEASES |
JP5546636B2 (en) | 2009-09-28 | 2014-07-09 | エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト | Benzoxepin PI3K inhibitor compounds and methods of use |
GB0919423D0 (en) | 2009-11-05 | 2009-12-23 | Glaxosmithkline Llc | Novel compounds |
CN102199152A (en) | 2010-03-25 | 2011-09-28 | 高大新 | Heterocycle imidazoles phosphatide kinases inhibitor |
CN102372711B (en) * | 2010-08-18 | 2014-09-17 | 山东轩竹医药科技有限公司 | Imidazo quinoline PI3K and mTOR (mammalian target of rapamycin) dual inhibitor |
US20120046272A1 (en) | 2010-08-23 | 2012-02-23 | Grunenthal Gmbh | Novel Therapeutic Compounds |
DE102010035744A1 (en) * | 2010-08-28 | 2012-03-01 | Merck Patent Gmbh | Imidazolonylchinoline |
CN102399218A (en) * | 2010-09-16 | 2012-04-04 | 和记黄埔医药(上海)有限公司 | Triheterocyclic compounds and their use as PI3K inhibitors |
AR083267A1 (en) | 2010-10-04 | 2013-02-13 | Novartis Ag | PHARMACEUTICAL COMBINATIONS |
MA34806B1 (en) | 2010-12-03 | 2014-01-02 | Novartis Ag | PHARMACEUTICAL COMPOSITIONS |
AU2011340167A1 (en) | 2010-12-06 | 2013-07-18 | Piramal Enterprises Limited | Substituted imidazoquinoline derivatives |
WO2012083866A1 (en) | 2010-12-22 | 2012-06-28 | The Hong Kong Polytechnic University | Quinoline derivatives as anti-cancer agents |
TWI450891B (en) | 2010-12-29 | 2014-09-01 | Dev Center Biotechnology | Novel tubulin inhibitors |
JO3003B1 (en) * | 2011-01-14 | 2016-09-05 | Lilly Co Eli | Imidazo [4,5-c] quinolin-2-one compound and its use as pi3 kinase i mtor dual inhibitor |
EP2694678A2 (en) | 2011-04-04 | 2014-02-12 | Netherland Cancer Institute | Methods and compositions for predicting resistance to anticancer treatment |
US9884828B2 (en) | 2011-05-23 | 2018-02-06 | Imago Pharmaceuticals, Inc. | Substituted cinnolines as inhibitors of LRRK2 kinase activity |
US10533000B2 (en) | 2011-05-26 | 2020-01-14 | Sunovion Pharmaceuticals, Inc. | Metabotrophic glutamate receptor 5 modulators and methods of use thereof |
WO2013022740A2 (en) | 2011-08-05 | 2013-02-14 | Corning Incorporated | Gpr35 ligands and the uses thereof |
JP6042060B2 (en) | 2011-09-26 | 2016-12-14 | サノフイ | Pyrazoloquinolinone derivatives, their preparation and therapeutic use |
EP2776437B1 (en) | 2011-11-07 | 2018-09-26 | Sunovion Pharmaceuticals Inc. | Modulators of opioid receptors and methods of use thereof |
WO2013074965A1 (en) | 2011-11-16 | 2013-05-23 | Microbiotix, Inc. | Aminoalkyl phenol ether inhibitors of influenza a virus |
WO2013157018A1 (en) | 2012-04-18 | 2013-10-24 | Indian Institute Of Technology Madras | A process for the preparation of the core structure in quinolone and napthyridone class of antibiotics |
CA2872541A1 (en) | 2012-06-06 | 2013-12-12 | Novartis Ag | Combination of a 17 -alpha -hydroxylase (c17, 20 - lyase) inhibitor and a specific pi-3k inhibitor for treating a tumor disease |
AU2013271731A1 (en) | 2012-06-07 | 2014-12-18 | Georgia State University Research Foundation, Inc. | SecA inhibitors and methods of making and using thereof |
WO2013192367A1 (en) | 2012-06-22 | 2013-12-27 | Novartis Ag | Neuroendocrine tumor treatment |
MX369518B (en) | 2012-08-16 | 2019-11-11 | Novartis Ag | Combination of pi3k inhibitor and c-met inhibitor. |
WO2014031872A2 (en) | 2012-08-23 | 2014-02-27 | The Broad Institute, Inc. | Small molecule inhibitors for treating parasitic infections |
EP2968348A4 (en) | 2013-03-12 | 2016-11-09 | Curegenix Inc | Compounds for treatment of cancer |
GB201309180D0 (en) | 2013-05-21 | 2013-07-03 | Ucl Business Plc | Compounds and Their Uses |
WO2015073804A2 (en) | 2013-11-15 | 2015-05-21 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Method of blocking transmission of malarial parasite |
EP3077393A1 (en) * | 2013-12-06 | 2016-10-12 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of atr kinase |
NO2714752T3 (en) * | 2014-05-08 | 2018-04-21 | ||
GB201409044D0 (en) | 2014-05-21 | 2014-07-02 | Ucl Business Plc | New compounds |
EP3560924B1 (en) | 2015-04-02 | 2021-03-31 | Merck Patent GmbH | Imidazolonyl quinolines and their use as atm kinase inhibitors |
CN104876912B (en) | 2015-04-08 | 2017-07-21 | 苏州云轩医药科技有限公司 | Wnt signal path inhibitor and its application |
US10858316B2 (en) | 2015-07-10 | 2020-12-08 | University Of Maryland, Baltimore | Small molecule inhibitors of the MCL-1 oncoprotein and uses thereof |
GB201516504D0 (en) * | 2015-09-17 | 2015-11-04 | Astrazeneca Ab | Imadazo(4,5-c)quinolin-2-one Compounds and their use in treating cancer |
MX2018011105A (en) | 2016-03-16 | 2018-11-22 | Kura Oncology Inc | Substituted inhibitors of menin-mll and methods of use. |
-
2015
- 2015-09-17 GB GBGB1516504.6A patent/GB201516504D0/en not_active Ceased
-
2016
- 2016-09-14 TW TW105129931A patent/TWI714631B/en active
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